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rs1064793481

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position28767982
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1064793481
dbSNP (old)rs1064793481
ClinGenrs1064793481
ebirs1064793481
HLIrs1064793481
Exacrs1064793481
Gnomadrs1064793481
Varsomers1064793481
Maprs1064793481
PheGenIrs1064793481
Biobankrs1064793481
1000 genomesrs1064793481
hgdprs1064793481
ensemblrs1064793481
gopubmedrs1064793481
geneviewrs1064793481
scholarrs1064793481
googlers1064793481
pharmgkbrs1064793481
gwascentralrs1064793481
openSNPrs1064793481
23andMers1064793481
23andMe allrs1064793481
SNPshotrs1064793481
SNPdbers1064793481
MSV3drs1064793481
GWAS Ctlgrs1064793481
Max Magnitude0
ClinVar
Risk rs1064793481(-;-)
Alt rs1064793481(-;-)
Reference Rs1064793481(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237188delC
CLNSRC
CLNACC RCV000485796.1,